Publications

[The evolution of epilepsy in the most common genetic forms with mental retardation (Down's syndrome and the fragile X syndrome)]., Guerrini, R., Dravet C., Ferrari A. R., Battaglia A., Mattei M. G., Salvadori P., Genton P., and Pfanner P. , La Pediatria medica e chirurgica : Medical and surgical pediatrics, 1993 May-Jun, Volume 15 Suppl 1, p.19-22, (1993) Abstract

[Reducing and stopping treatment]., Roger, J., Guerrini R., and Genton P. , La Revue du praticien, 1990 Feb 1, Volume 40, Issue 4, p.323-7, (1990) Abstract

[Psychopathological risk in children with early onset of partial epilepsy]., Bargagna, S., Guerrini R., and Millepiedi S. , Minerva pediatrica, 1995 May, Volume 47, Issue 5, p.193-7, (1995) Abstract

[Partial trisomy of the long arm of chromosome 6. A clinical case]., Dellacasa, P., Bonanni P., and Guerrini R. , Minerva pediatrica, 1993 Dec, Volume 45, Issue 12, p.517-21, (1993) Abstract

[Contribution of ambulatory EEG recording (Medilog 9000) in a population of epileptics]., Bureau, M., Guerrini R., Vigliano P., and Dravet C. , Neurophysiologie clinique = Clinical neurophysiology, 1989 Jun, Volume 19, Issue 3, p.219-30, (1989) Abstract

X-linked malformations of neuronal migration., Dobyns, W. B., Andermann E., Andermann F., Czapansky-Beilman D., Dubeau F., Dulac O., Guerrini R., Hirsch B., Ledbetter D. H., Lee N. S., et al. , Neurology, 1996 Aug, Volume 47, Issue 2, p.331-9, (1996) Abstract

What differentiates Landau-Kleffner syndrome from the syndrome of continuous spikes and waves during slow sleep?, Genton, P., and Guerrini R. , Archives of neurology, 1993 Oct, Volume 50, Issue 10, p.1008-9, (1993)

Trisomy 12p syndrome: a chromosomal disorder associated with generalized 3-Hz spike and wave discharges., Guerrini, R., Bureau M., Mattei M. G., Battaglia A., Galland M. C., and Roger J. , Epilepsia, 1990 Sep-Oct, Volume 31, Issue 5, p.557-66, (1990) Abstract

Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients., Gambardella, A., Aguglia U., Guerrini R., Morelli F., Zappia M., and Quattrone A. , Brain & development, 1996 May-Jun, Volume 18, Issue 3, p.212-5, (1996) Abstract

Reversible pseudoatrophy of the brain and mental deterioration associated with valproate treatment., Guerrini, R., Belmonte A., Canapicchi R., Casalini C., and Perucca E. , Epilepsia, 1998 Jan, Volume 39, Issue 1, p.27-32, (1998) Abstract

Reflex seizures are frequent in patients with Down syndrome and epilepsy., Guerrini, R., Genton P., Bureau M., Dravet C., and Roger J. , Epilepsia, 1990 Jul-Aug, Volume 31, Issue 4, p.406-17, (1990) Abstract

Periventricular nodular heterotopia in Smith-Magenis syndrome., Capra, Valeria, Biancheri Roberta, Morana Giovanni, Striano Pasquale, Novara Francesca, Ferrero Giovanni Battista, Boeri Luca, Celle Maria Elena, Mancardi Maria Margherita, Zuffardi Orsetta, et al. , American journal of medical genetics. Part A, 2014 Dec, Volume 164A, Issue 12, p.3142-7, (2014) Abstract

Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritance., Guerrini, R., Belmonte A., and Carrozzo R. , Brain & development, 1998 Mar, Volume 20, Issue 2, p.116-8, (1998) Abstract

Panic attacks mistaken for relapse of epilepsy., Genton, P., Bartolomei F., and Guerrini R. , Epilepsia, 1995 Jan, Volume 36, Issue 1, p.48-51, (1995) Abstract

Occipitotemporal seizures with ictus emeticus induced by intermittent photic stimulation., Guerrini, R., Ferrari A. R., Battaglia A., Salvadori P., and Bonanni P. , Neurology, 1994 Feb, Volume 44, Issue 2, p.253-9, (1994) Abstract

Neurological findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRI., Guerrini, R., Dravet C., Raybaud C., Roger J., Bureau M., Battaglia A., Livet M. O., Colicchio G., and Robain O. , Developmental medicine and child neurology, 1992 Aug, Volume 34, Issue 8, p.694-705, (1992) Abstract

Myoclonic absence-like seizures and chromosome abnormality syndromes., Elia, M., Guerrini R., Musumeci S. A., Bonanni P., Gambardella A., and Aguglia U. , Epilepsia, 1998 Jun, Volume 39, Issue 6, p.660-3, (1998) Abstract

Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency., Tan, Chuan, Shard Chloe, Ranieri Enzo, Hynes Kim, Pham Duyen H., Leach Damian, Buchanan Grant, Corbett Mark, Shoubridge Cheryl, Kumar Raman, et al. , Human molecular genetics, 2015 Jun 29, (2015) Abstract

Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome., Doccini, Stefano, Meschini Maria Chiara, Mei Davide, Guerrini Renzo, Sicca Federico, and Santorelli Filippo Maria , Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2015 Jul 14, (2015)

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain., Ross, M. E., Allen K. M., Srivastava A. K., Featherstone T., Gleeson J. G., Hirsch B., Harding B. N., Andermann E., Abdullah R., Berg M., et al. , Human molecular genetics, 1997 Apr, Volume 6, Issue 4, p.555-62, (1997) Abstract